Results 81 to 90 of about 130,822 (183)

Development of Human Carbonic Anhydrase II Heterobifunctional Degraders. [PDF]

open access: yesJ Med Chem, 2023
O'Herin CB   +5 more
europepmc   +1 more source

Carbonic Anhydrase II Deficiency in a Saudi Woman

open access: yesClinical Medicine Insights: Case Reports, 2015
Objective Carbonic anhydrase (CA) II deficiency is a rare autosomal recessive disorder caused by mutation in the CA II gene that leads to osteopetrosis, renal tubular acidosis (RTA), and cerebral calcification.
Omar N. Alhuzaim   +2 more
doaj   +1 more source

Novel pyrazole-3,4-dicarboxamides bearing biologically active sulfonamide moiety as potential carbonic anhydrase inhibitors

open access: yesArabian Journal of Chemistry, 2019
In this study a series of pyrazole-3,4-dicarboxamide (3–10) derivatives bearing sulfonamide moiety were synthesized starting from 1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3,4-dicarboxylic acid (1). The structures of synthesized molecules were characterized
Samet Mert   +5 more
doaj  

Clinical Characteristics and Mutation Profile in Patients with Carbonic Anhydrase II Deficiency: A Systematic Review of Case Reports

open access: yesIndian Pediatrics Case Reports
Background: Carbonic anhydrase II (CA II) deficiency is a rare autosomal recessive genetic disorder presenting with the characteristic triad of osteopetrosis, renal tubular acidosis (RTA), and intracerebral calcifications.
Rajkumar Kundavaram   +6 more
doaj   +1 more source

High-activity carbonic anhydrase isoenzyme (CA II) in human gallbladder epithelium. [PDF]

open access: bronze, 1994
Tatu Juvonen   +7 more
openalex   +1 more source

Biochemical and in silico inhibition of bovine and human carbonic anhydrase-II by 1H-1,2,3-triazole analogs. [PDF]

open access: yesFront Chem, 2022
Khan M   +6 more
europepmc   +1 more source

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